Gene entry
SLC13A5
solute carrier family 13 member 5
- Chromosome
- 17
- Cytoband
- 17p13.1
- Variants (rsID)
- 20
SLC13A5 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 17 (region 17p13.1). Its official name is “solute carrier family 13 member 5”. The reference table lists 20 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
- rs773770609Pathogenicsingle nucleotide variantDevelopmental and epileptic encephalopathy, 25|Seizure
- rs182042247Uncertain significancesingle nucleotide variantDevelopmental and epileptic encephalopathy, 25
Other listed variants
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.